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Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease

INTRODUCTION: Olfactory dysfunction affects about 85-90% of Parkinson's disease (PD) patients with severe deterioration in the ability of discriminate several types of odors. In addition, studies reported declines in olfactory performances during a short period of sleep deprivation. Besides, PD...

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Autores principales: Aurich, Mariana F., Rodrigues, Lais S., Targa, Adriano D. S., Noseda, Ana Carolina D., Cunha, Flávia D. W., Lima, Marcelo M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Association of Sleep and Latin American Federation of Sleep 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611772/
https://www.ncbi.nlm.nih.gov/pubmed/28966738
http://dx.doi.org/10.5935/1984-0063.20170008
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author Aurich, Mariana F.
Rodrigues, Lais S.
Targa, Adriano D. S.
Noseda, Ana Carolina D.
Cunha, Flávia D. W.
Lima, Marcelo M. S.
author_facet Aurich, Mariana F.
Rodrigues, Lais S.
Targa, Adriano D. S.
Noseda, Ana Carolina D.
Cunha, Flávia D. W.
Lima, Marcelo M. S.
author_sort Aurich, Mariana F.
collection PubMed
description INTRODUCTION: Olfactory dysfunction affects about 85-90% of Parkinson's disease (PD) patients with severe deterioration in the ability of discriminate several types of odors. In addition, studies reported declines in olfactory performances during a short period of sleep deprivation. Besides, PD is also known to strongly affect the occurrence and maintenance of rapid eye movement (REM) sleep. METHODS: Therefore, we investigated the mechanisms involved on discrimination of a social odor (dependent on the vomeronasal system) and a non-social odor (related to the main olfactory pathway) in the rotenone model of PD. Also, a concomitant impairment in REM sleep was inflicted with the introduction of two periods (24 or 48 h) of REM sleep deprivation (REMSD). Rotenone promoted a remarkable olfactory impairment in both social and non-social odors, with a notable modulation induced by 24 h of REMSD for the non-social odor. RESULTS: Our findings demonstrated the occurrence of a strong association between the density of nigral TH-ir neurons and the olfactory discrimination capacity for both odorant stimuli. Specifically, the rotenone-induced decrease of these neurons tends to elicit reductions in the olfactory discrimination ability. CONCLUSIONS: These results are consistent with the participation of the nigrostriatal dopaminergic system mainly in the olfactory discrimination of a non-social odor, probably through the main olfactory pathway. Such involvement may have produce relevant impact in the preclinical abnormalities found in PD patients.
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spelling pubmed-56117722017-09-29 Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease Aurich, Mariana F. Rodrigues, Lais S. Targa, Adriano D. S. Noseda, Ana Carolina D. Cunha, Flávia D. W. Lima, Marcelo M. S. Sleep Sci Original Article INTRODUCTION: Olfactory dysfunction affects about 85-90% of Parkinson's disease (PD) patients with severe deterioration in the ability of discriminate several types of odors. In addition, studies reported declines in olfactory performances during a short period of sleep deprivation. Besides, PD is also known to strongly affect the occurrence and maintenance of rapid eye movement (REM) sleep. METHODS: Therefore, we investigated the mechanisms involved on discrimination of a social odor (dependent on the vomeronasal system) and a non-social odor (related to the main olfactory pathway) in the rotenone model of PD. Also, a concomitant impairment in REM sleep was inflicted with the introduction of two periods (24 or 48 h) of REM sleep deprivation (REMSD). Rotenone promoted a remarkable olfactory impairment in both social and non-social odors, with a notable modulation induced by 24 h of REMSD for the non-social odor. RESULTS: Our findings demonstrated the occurrence of a strong association between the density of nigral TH-ir neurons and the olfactory discrimination capacity for both odorant stimuli. Specifically, the rotenone-induced decrease of these neurons tends to elicit reductions in the olfactory discrimination ability. CONCLUSIONS: These results are consistent with the participation of the nigrostriatal dopaminergic system mainly in the olfactory discrimination of a non-social odor, probably through the main olfactory pathway. Such involvement may have produce relevant impact in the preclinical abnormalities found in PD patients. Brazilian Association of Sleep and Latin American Federation of Sleep 2017 /pmc/articles/PMC5611772/ /pubmed/28966738 http://dx.doi.org/10.5935/1984-0063.20170008 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivative License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way.
spellingShingle Original Article
Aurich, Mariana F.
Rodrigues, Lais S.
Targa, Adriano D. S.
Noseda, Ana Carolina D.
Cunha, Flávia D. W.
Lima, Marcelo M. S.
Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease
title Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease
title_full Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease
title_fullStr Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease
title_full_unstemmed Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease
title_short Olfactory impairment is related to REM sleep deprivation in rotenone model of Parkinson's disease
title_sort olfactory impairment is related to rem sleep deprivation in rotenone model of parkinson's disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611772/
https://www.ncbi.nlm.nih.gov/pubmed/28966738
http://dx.doi.org/10.5935/1984-0063.20170008
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